What We Are Trying to Accomplish
MS is an expensive disease, with the average direct and indirect expenses (e.g. healthcare costs, lost wages), averaging upwards of $70,000 per year, per person. People living with MS and their families are increasingly concerned with their ability to afford medications and necessities such as food and housing. The Society recognizes that managing MS includes more than just the costs of a disease modifying and symptom management therapies. To support people with MS in all aspects of their lives, the Society’s policy work includes addressing issues around employment, transportation, housing, access to adequate nutrition and addressing health disparities that impact diagnosis, care and treatment. We work at the state and federal level to reduce the direct financial impact of MS and ensure everyone living with MS can live their best lives.
Most people with MS are diagnosed between the ages of 20 and 50—prime working years. Although most people with MS have a work history, and labor force participation comparable to that of the general population at the time of diagnosis, the ability of people with MS to remain in the work force declines steadily with disease progression, which can negatively impact an individual’s finances, access to healthcare and more.
Help reduce the direct financial impact of MS.
Interested in taking action nearby? Simply filter by state and see what you can do in your area.